|
341
|
|
|
Clavesin 2 |
C6orf212, C6orf213, RLBP1L2, bA160A10.4 |
|
|
342
|
|
|
Cytochrome c oxidase subunit 7B |
APLCC, LSDMCA2 |
Absence of septum pellucidum, Agenesis of corpus callosum, Ambiguous genitalia, Aphasia, Aplasia cutis congenita, Atrial septal defect, Cardiomyopathy, Cataract, Colpocephaly, Mandibular aplasia, Congenital anomaly of rectum, Congenital coloboma of iris, Congenital diaphragmatic hernia, Developmental delay, Dwarfism, Dysphasia, Epispadias, Glaucoma, Heart septal defects, Histiocytoid cardiomyopathy, Hydrocephalus, Hypertrophic cardiomyopathy, Hypertrophy of clitoris, Hypospadias, Imperforate anus, Linear skin defects with multiple congenital anomalies, Male pseudohermaphroditism, Mental retardation, Microcephaly, Micrognathism, Microphthalmia with linear skin defects syndrome, Syndromic microphthalmia, Microphthalmos, Mitral valve prolapse, Overriding aorta, Ovotestis, Penis agenesis, Posterior embryotoxon, Respiratory failure, Retinal dysplasia, Retinal dystrophy, Retinitis pigmentosa, Sclerocornea, Specific learning disorder, Status epilepticus, Tricuspid valve insufficiency, Tricuspid valve prolapse, True hermaphroditism, Ventricular septal defect, VitritisView all (35 more) |
|
343
|
|
|
Cytochrome c oxidase subunit 7C |
- |
|
|
344
|
|
|
Cytochrome c oxidase subunit 8A |
COX, COX8, COX8-2, COX8L, MC4DN15, VIII, VIII-L |
Anemia, Cytochrome-c oxidase deficiency, Developmental delay, Fanconi syndrome, Hearing loss, High palate, Hypertrophic cardiomyopathy, Isolated cytochrome c oxidase deficiency, Leukoencephalopathy, Mental retardation, Motor delay, Optic atrophy, Phosphate diabetes, Ptosis, Renal tubular disorder, Retinitis pigmentosaView all (1 more) |
|
345
|
|
|
Cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 |
MC4DN3 |
Anemia, Central nervous system demyelination, Cytochrome-c oxidase deficiency, Developmental delay, Dysarthria, Encephalopathy, Fanconi syndrome, Hearing loss, High palate, Hypertrichosis, Hypertrophic cardiomyopathy, Isolated cytochrome c oxidase deficiency, Leigh syndrome, Leukoencephalopathy, Mental retardation, Mitochondrial diseases, Mood swings, Motor delay, Necrotizing encephalomyelopathy, Nystagmus, Optic atrophy, Phosphate diabetes, Ptosis, Renal tubular disorder, Respiratory failure, Retinitis pigmentosa, StrabismusView all (12 more) |
|
346
|
|
|
CD109 molecule |
CPAMD7, p180, r150 |
Alloimmune thrombocytopenia, Breast cancer, Mammary neoplasms, Breast carcinoma, Cerebral palsy, Colorectal cancer, Colorectal neoplasms, Developmental delay, Fetal and neonatal alloimmune thrombocytopenia, Hematomas, Marfan syndrome, Sensorineural hearing loss, Subarachnoid hemorrhage |
|
347
|
|
|
Cytochrome c oxidase assembly factor COX15 |
CEMCOX2, HAS, MC4DN6 |
Anemia, Cardioencephalomyopathy, Cardiomyopathy, Central nervous system demyelination, Cerebellar ataxia, Cytochrome-c oxidase deficiency, Developmental delay, Dysarthria, Encephalopathy, Epileptic encephalopathy, Fatal cytochrome c oxidase deficiency, Fatty liver, Hearing loss, Hypertrichosis, Hypertrophic cardiomyopathy, Mental retardation, Leigh syndrome, Leigh syndrome with leukodystrophy, Leukodystrophy, Microcephaly, Mitochondrial diseases, Mood swings, Necrotizing encephalomyelopathy, Nervous system diseases, Nystagmus, Optic atrophy, Ptosis, Respiratory failure, Retinitis pigmentosa, Strabismus, Ventricular septal defectView all (16 more) |
|
348
|
|
|
Ceruloplasmin |
AB073614, CP-2 |
Aceruloplasminemia, Anemia, Apoceruloplasmin deficiency, Autism, Autoimmune diabetes, Ballismus, Blepharospasm, Ceruloplasmin deficiency, Colonic neoplasms, Congestive heart failure, Dementia, Diabetes mellitus, Brittle diabetes mellitus, Dysarthria, Dyskinetic syndrome, Epileptic encephalopathy, Hemiballismus, Hemochromatosis, Systemic hemosiderosis, Hepatolenticular degeneration, Hereditary hemochromatosis, Hermansky-pudlak syndrome, Hypothyroidism, Iron metabolism disorders, Iron overload, Kidney failure, Leukemia, Orofacial dyskinesia, Liver carcinoma, Liver cirrhosis, Liver fibrosis, Melanoma, Menkes kinky hair syndrome, Mental depression, Movement disorders, Oral dyskinesia, Palmoplantar pustules, Parkinson disease, Psoriasis, Acute kidney insufficiency, Rheumatoid arthritis, Rubral tremor, Schizophrenia, Senile paranoid dementiaView all (29 more) |
|
349
|
|
|
Carboxypeptidase A1 |
CPA |
|
|
350
|
|
|
Carboxypeptidase A2 |
- |
|
